Classifications

• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K5/00—Use of organic ingredients
  • C08K5/04—Oxygen-containing compounds
  • C08K5/06—Ethers; Acetals; Ketals; Ortho-esters
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K5/00—Use of organic ingredients
  • C08K5/04—Oxygen-containing compounds
  • C08K5/10—Esters; Ether-esters
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
  • C09K3/00—Materials not provided for elsewhere
  • C09K3/18—Materials not provided for elsewhere for application to surfaces to minimize adherence of ice, mist or water thereto; Thawing or antifreeze materials for application to surfaces
• • D—TEXTILES; PAPER
  • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
  • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
  • D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
  • D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
  • D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
  • D06M15/263—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acids; Salts or esters thereof
  • D06M15/277—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acids; Salts or esters thereof containing fluorine
• • D—TEXTILES; PAPER
  • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
  • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
  • D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
  • D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
  • D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
  • D06M15/285—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acid amides or imides
• • D—TEXTILES; PAPER
  • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
  • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
  • D06M2200/00—Functionality of the treatment composition and/or properties imparted to the textile material
  • D06M2200/10—Repellency against liquids
  • D06M2200/11—Oleophobic properties
• • D—TEXTILES; PAPER
  • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
  • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
  • D06M2200/00—Functionality of the treatment composition and/or properties imparted to the textile material
  • D06M2200/10—Repellency against liquids
  • D06M2200/12—Hydrophobic properties

Definitions

• the present invention relates to a novel composition, a water and oil repellent and a water and oil repellent product.
• a conventional water and oil repellent required a heat treatment at 100°C or more as an essential step to impart high water and oil repellency, but various water and oil repellents have been proposed to improve processability of the water and oil repellents.
• Japanese Patent Kokoku Publication No. 67511/1988 discloses a polymer obtained by binding a branch segment having a blocked fluoroalkyl group to a trunk segment of a diene copolymer
• Japanese Patent Kokai Publication No.71977/1983 discloses that a copolymer comprising a monomer having a fluoroalkyl group and a cross-linking monomer as an essential component is a water and oil repellent which imparts high water and oil repellency in a heat treatment step at low temperature. However, when both of them are dried at room temperature, the water and oil repellency is insufficient.
• U.S. Patent No. 5,350,795 discloses that a composition comprising fluoroacrylate/ polyalkyleneglycol (meth)acrylate/ polyalkyleneglycol di(meth)acrylate copolymer and Rf-containing polyalkoxypolyurethane is a water and oil repellent which imparts high water and oil repellency when it is dried at room temperature.
• the water repellency is insufficient.
• a conventional water and oil repellent requires a heat treatment as an essential step to impart high water and oil repellency, and sufficient water and oil repellency could not be imparted without a heat treatment.
• An object of the present invention is to provide a composition which imparts high water and oil repellency only by drying at room temperature (0 to 30°C) without requiring a heat treatment step.
• Another object of the present invention is to provide a water and oil repellent product or article comprising said composition.
• the present invention provides a composition comprising
• Repeating units (1) which impart water and oil repellency may be (I) repeating units which are derived from a monomer having a fluoroalkyl group, a carbon-carbon double bond, and optionally a urethane or urea bond.
• Repeating units (2) which impart solubility in (or compatibility with) a film-forming auxiliary may be (II) repeating units which are derived from a monomer having a urethane or urea bond and a carbon-carbon double bond, but no fluorine atom; or (III) repeating units which are derived from a monomer having a carbon-carbon double bond, the homopolymer of said monomer having a glass transition temperature (Tg) of at most 50°C.
• Tg glass transition temperature
• Repeating units (3) which lower the glass transition temperature of the polymer may be (III) repeating units which are derived from a monomer having a carbon-carbon double bond, the homopolymer of said monomer having a glass transition temperature (Tg) of at most 50°C.
• Repeating units (4) which impart an affinity with a substrate may be (IV) repeating units which are derived from a monomer having a hydrophilic group and a carbon-carbon double bond, or (V) repeating units which are derived from a monomer having a chlorine atom and a carbon-carbon double bond.
• the present invention provides a composition comprising
• composition of the present invention is suitable for a treatment agent, in particular a water and oil repellent.
• the repeating units (I) are essential in the copolymer (A).
• the repeating units (II), the repeating units (III), the repeating units (IV) and the repeating units (V) are optional repeating units which have no need to be present. But at least one of the repeating units (II) and the repeating units (III) is essential.
• copolymer (A) in the composition of the present invention may be, for example:
• the present invention provides a copolymer wherein the repeating units (I), the repeating units (II) and the repeating units (III) are essential, and the repeating units (IV) and the repeating units (V) are optional.
• a fluoroalkyl group is preferably a perfluoroalkyl group.
• the repeating units (I) are preferably repeating units which are derived from (meth)acrylic ester containing a fluoroalkyl group.
• Examples of the monomer (I) having a fluoroalkyl group are not limited to, but include the followings:
• a monomer having a urethane or urea bond and a fluoroalkyl group, which constitutes the repeating units (I), may be a monomer obtained by reacting
• the monomer (II) having a urethane or urea bond and a carbon-carbon double bond, but no fluorine atom may be a monomer obtained by reacting
• the compound (II-a) is preferably diisocyanate. But triisocyanate and polyisocyanate can be also used for the reaction.
• a trimer of diisocyanate, polymeric MDI (diphenylmethanediisocyanate) as well as an adduct of polyhydric alcohols such as trimethylol propane, trimethylol ethane and glycerin to a diisocyanate can be also used in the reaction.
• triisocyanate and polyisocyanate are as follows:
• the compound (II-b) may be, for example, a compound of the formula: wherein R 1 is a hydrogen atom or a methyl group, p is a number of 1 to 300 (e.g. 1 to 20) and X is as follows: wherein p, m and n are a number of 1 to 300, respectively.
• the compound (II-c-1) may be a compound of the formula: wherein R 1 represents a hydrogen atom or a C 1 to C 22 alkyl group, in the latter case a hetero atom, or an aromatic or an alicyclic compound may be contained; R 2 represents a liner or branched C 1 to C 6 alkylene group; R 3 and R 4 represents a hydrogen atom or a C 1 to C 6 alkyl group which optionally contains a hetero atom, or an aromatic or an alicyclic compound, or optionally contains a modification such as fluorine modification, polyether modification, alcohol modification, amino modification, epoxy modification, epoxy ether modification, phenol modification, carboxyl modification, and mercapto modification; and n represents an integer of 1 to 50.
• Preferred R 1 , R 3 and R 4 groups are CH 3 and preferred R 2 group is C 2 H 4 and C 3 H 6 .
• Examples of the compound (II-c-1) are polyethylene glycol monomethyl ether, polypropylene glycol monomethyl ether, end silanol group dimethyl silicone and end amino-modified dimethyl silicone.
• the compound (II-c-2) has neither of a polyoxyalkylene chain nor a polysiloxane chain.
• the compound (II-c-2) may be a compound of the formula: R 2 -OH R 2 -NH 2 or R 2 -NH-R 3 wherein R 2 and R 3 , the same or different, represent a C 1 , to C 22 alkyl group and optionally contain a hetero atom, or an aromatic or an alicyclic compound.
• Preferred R 2 and R 3 groups are C 8 H 17 , C 18 H 37 , C 4 H 9 and cyclohexyl.
• Examples of the compound (II-c-2) include butyl alcohol, 2-ethylhexyl alcohol, lauryl alcohol, stearyl alcohol, oleyl alcohol, benzyl alcohol, cyclohexyl alcohol, 2-ethylhexylamine and stearylamine.
• the compound (II-a), (II-b) and (II-c-1) or (II-c-2) are reacted in amounts of; when (II-a) is diisocyanate, one mol of(II-b) and (II-c-1) or (II-c-2) per one mol of(II-a), and when (II-a) is triisocyanate, one mol of (II-b) and two mols of(II-c-1) or (II-c-2) per one mol of(II-a).
• a monomer which constitutes the repeating units (III) may be a monomer having conjugated double bonds or one or two carbon-carbon double bonds, and a glass transition temperature (Tg) of 50°C or less, for example 30°C or less, particularly 0°C or less.
• Tg glass transition temperature
• a monomer having a glass transition temperature (Tg) of 50°C or less means that the homopolymer consisting of said monomer has a glass transition temperature (Tg) of 50°C or less.
• Tg was measured by using DSC, Model 7 manufactured by Perkin Elmer Co.
• a monomer which constitutes the repeating units (III) is preferably a diene monomer, a (meth)acrylic ester monomer or a di(meth)acrylic ester monomer.
• Examples of the monomer having a glass transition temperature of 30 to 50°C include cetyl acrylate and isobutyl methacrylate for examples of the (meth)acrylic ester monomer; and polyethylene glycol(4)diacrylate for examples of the di(meth)acrylic ester monomer.
• Examples of the monomer having a glass transition temperature of 0 to 30°C include methyl acrylate, n-butyl methacrylate, and cetyl methacrylate for examples of the (meth)acrylic ester monomer.
• Examples of the monomer having a glass transition temperature of 0°C or less include isoprene and 1,3-butadiene for examples of the diene monomer; and ethyl acrylate, n-butyl acrylate, n-octyl acrylate, 2-ethylhexyl (meth)acrylate, n-lauryl (meth)acrylate for examples of the (meth)acrylic ester monomer.
• hydrophilic group examples include a hydroxyl group, a glycidyl group, an ester group, an amine group, a urethane group, a phosphate group, a sulfate group and the like.
• Examples of the monomer which constitutes the repeating units (IV) include glycidyl methacrylate, hydroxypropyl methacrylate, 2-hydroxy-3-phenoxypropyl acrylate, 2-hydroxyethyl acrylate, glycerol monomethacrylate, ⁇ -acryloyloxyethyl hydrogen succinate, ⁇ -methacryloyloxyethyl hydrogen phthalate, 2-acryloyloxyethylhexahydrophthalic acid, 2-acryloyloxyethylphthalic acid, 2-acryloyloxyethyl-2-hydroxyethylphthalic acid, hydroxypropyl methacrylate trimethylammonium chloride, dimethylaminoethyl methacrylate, diethylaminoethyl methacrylate, 2-acryloyloxyethyl acid phosphate, glucosylethyl methacrylate, methacrylamide, 2-acrylamido-2-methylpropanesulfonic acid,
• chlorine-containing monomer which constitutes the repeating units (V) examples include vinyl chloride, vinylidene chloride, 3-chloro-2-hydroxypropyl methacrylate and monochlorotrifluoroethylene.
• a weight average molecular weight of the copolymer (A) is preferably from 2,000 to 1,000,000.
• the amount of the repeating units (I) is preferably from 40 to 90% by weight, and more preferably from 50 to 80% by weight,
• the film-forming auxiliary (B) which facilitates the film-forming of the copolymer (A) by existing together with the copolymer (A) is preferably those which dissolves, swells or softens the copolymer (A).
• the film-forming auxiliary (B) may be (i) an alcohol, glycol ether, ketone, ether and ester having a C 1 to C 22 alkyl chain, or (ii) a linear or cyclic silicone.
• the film-forming auxiliary (B) (i) may be a compound containing a fluorine atom, a hetero atom, an aromatic ring or an aliphatic ring.
• the film-forming auxiliary (B) (ii) may be a compound of the formula: wherein R 9 and R 10 each represents a hydrogen atom or a C 1 to C 6 alkyl group, which optionally contains a hetero atom, an aromatic or an alicyclic compound, or optionally contains a modification such as fluorine modification, polyether modification, alcohol modification, amino modification, epoxy modification, epoxy ether modification, phenol modification, carboxyl modification and mercapto modification; and n represents a number of 1 to 50.
• solubility parameter As the film-forming auxiliary (B), a compound having the value of the solubility parameter (sp) at 25°C of 5 to 15, e.g. 8 to 11 is suitable.
• the solubility parameter is calculated according to Fedors' method (R.F. Fedors, Polym. Eng. Sci., 14(2), 147(1974)).
• the role of the film-forming auxiliary is to dissolve, swell or soften the copolymer (A) and induce film-formation of the copolymer (A) with a low calorie. This makes it possible to impart high water and oil repellency without requiring any heat treatment step.
• the film-forming auxiliary may be single compound or two or more of them may be used in combination.
• the film-forming auxiliary may be the same as or different from the polymerization solvent.
• film-forming auxiliary (B) examples include, for example, ethanol, dipropylene glycol monomethyl ether, 1-methoxy-2-propanol, diethylene glycol acetate monoethyl ether, di-n-butyl adipate, butyl carbitol acetate, octamethyltrisiloxane and decamethylcyclopentasiloxane.
• composition of the present invention may comprise 30 to 99.9 parts by weight, particularly 40 to 95 parts by weight, e.g. 50 to 80 parts by weight of the copolymer (A) and 0.1 to 70 parts by weight, particularly 5 to 60 parts by weight, e.g. 20 to 50 parts by weight of the film-forming auxiliary (B).
• the copolymer can be prepared by emulsion polymerization, solution polymerization or suspension polymerization. In particular, the emulsion polymerization is preferred.
• the copolymer of the present invention can also be produced in an aqueous emulsion.
• Monomers are emulsion-polymerized by use of water, an emulsifying agent and optionally an organic solvent.
• the film-forming auxiliary (B) may be added before or after the emulsion polymerization.
• the mixture may previously be emulsified by a high-pressure emulsifying machine or the like before polymerization.
• the emulsifying agent used may be any type of a surface active agent, such as an anionic, cationic or nonionic surface active agent.
• anionic surface active agent examples include sodium lauryl sulfate, lauryl sulfate triethanolamine, sodium polyoxyethylene lauryl ether sulfate, sodium polyoxyethylene nonyl phenyl ether sulfate, polyoxyethylene lauryl ether sulfate triethanolamine, sodium cocoyl sarcosine, sodium N-cocoyl methyl taurine, sodium polyoxyethylene coconut alkyl ether sulfate, sodium diether hexyl sulfosuccinate, sodium ⁇ -olefin sulfonate, sodium lauryl phosphate, sodium polyoxyethylene lauryl ether phosphate, and perfluoroalkyl carboxylate salt (Unidine DS-101 and 102 manufactured by Daikin Industries Ltd.).
• cationic surface active agent examples include dialkyl (C 12 -C 22 ) dimethyl ammonium chloride, alkyl (coconut) dimethyl benzyl ammonium chloride, octadecyl amine acetate salt, tetradecyl amine acetate salt, tallow alkyl propylene diamine acetate salt, octadecyl trimethyl ammonium chloride, alkyl (tallow) trimethyl ammonium chloride, dodecyl trimethyl ammonium chloride, alkyl (coconut) trimethyl ammonium chloride, hexadecyl trimethyl ammonium chloride, behenyl trimethyl ammonium chloride, alkyl (tallow) imidazoline quaternary salt, tetradecyl methyl benzyl ammonium chloride, octadecyl dimethyl benzyl ammonium chloride, dioleyl dimethyl ammonium chloride, poly
• nonionic surface active agent examples include polyoxyethylene lauryl ether, polyoxyethylene tridecyl ether, polyoxyethylene cetyl ether, polyoxyethylene polyoxypropylene cetyl ether, polyoxyethylene stearyl ether, polyoxyethylene oleyl ether, polyoxyethylene nonyl phenyl ether, polyoxyethylene octyl phenyl ether, polyoxyethylene monolaurate, polyoxyethylene monostearate, polyoxyethylene monooleate, sorbitan monolaurate, sorbitan monostearate, sorbitan monopalmitate, sorbitan monostearate, sorbitan mono-oleate, sorbitan sesqui-oleate, sorbitan trioleate, polyoxyethylene sorbitan monolaurate, polyoxyethylene sorbitan monopalmitate, polyoxyethylene sorbitan monostearate, polyoxyethylene sorbitan mono-oleate, polyoxyethylene polyoxypropylene block polymer, polygly
• Examples of the organic solvent used in the emulsion polymerization are the same as the organic solvent used in the solution polymerization described hereinafter.
• the copolymer of present invention can be produced by the solution polymerization in an organic solvent.
• organic solvent include ketones such as acetone, methyl ethyl ketone and methyl isobutyl ketone; esters such as ethyl acetate, propyl acetate, butyl acetate, dibutyl adipate and dibutyl succinate; alcohols such as ethanol, isopropanol, butanol, 1,3-butanediol and 1,5-pentanediol; halogenated hydrocarbon such as perchlorethylene, trichlene, 1,1-dichloro-2,2,3,3,3-pentafluoropropane, 1,3-dichloro-1,2,2,3,3,3-pentafluoropropane and 1,1-dichloro-1-fluoroethane (HCFC-141b); hydrocarbons such as octane, petroleum, toluene and xylene
• the preferred organic solvents are ketones such as methyl ethyl ketone and methyl isobutyl ketone; ethyl acetate, 1,1-dichloro-1-fluoroethane and the like.
• a polymerization initiator In polymerization, a polymerization initiator, an ionizing radiation such as ⁇ -ray and the like is used to initiate the polymerization.
• the polymerization initiator are an organic peroxide, an azo compound, a persulfate salt and the like.
• Examples of the organic peroxide include t-butyl peroxy pivalate, benzoyl peroxide, lauroyl peroxide, di-t-butyl peroxide and diisopropyl peroxy dicarbonate.
• Examples of the azo compound include 2,2'-azobisisobutyronitrile, 2,2'-azobis(2-amidinopropane)dihydrochloride, 2,2'-azobis(2-methyl butaneamidooxime)dihydrochloride and 2,2'-azobis(2-methylbutyronitrile).
• the copolymer of the present invention can be used as a treatment agent.
• the treatment agent may be a water and oil repellent.
• the treatment agent comprises the copolymer and the film-forming auxiliary, an optional polymerization solvent and diluting solvent.
• the diluting solvent may be water, an alcohol (e.g. alkanol), a ketone, an ester, an ether (e.g. a glycol ether) or a mixture of them.
• the diluting solvent is preferably water.
• the film-forming auxiliary, the diluting solvent and the polymerization solvent may be different one another. When the diluting solvent and the polymerization solvent are different each other, the polymerization solvent may be removed (by evaporation, etc.) before using the treatment agent.
• the alcohol used as the diluting solvent includes C 1 to C 4 lower alkanols such as methanol, ethanol, 2-propanol and n-butanol. Among these lower alkanols, ethanol and 2-propanol are preferable in view of safety. Alkanols having at least five carbon atoms are not preferable because of poor drying characteristics. These lower alkanols can be used singly or in combination thereof.
• Solvents such as isoparaffin, n-heptane, n-hexane, mineral terpene, ethyl acetate, toluene, methyl ethyl ketone and methyl isobutyl ketone can be added at a less dangerous level.
• An alternative fluorocarbon such as fluorocarbon 141b can also be used as a matter of course.
• the addition of a small amount of glycol ethers such as dipropylene glycol monomethyl ether is also effective in preventing whitening.
• an organopolysiloxane is important because it can improve water repellency.
• the organopolysiloxane used may be a silicone oil, a silicone dispersion or a mixture thereof.
• the silicone oil is most typically dimethyl polysiloxane having various degrees of polymerization at a viscosity ranging from 0.65 to 300,000 cS at 25°C, which is represented by the following formula:
• a main chain of some organopolysiloxanes may contain a small amount of the following group:
• organopolysiloxanes may have the terminal of the main chain Si-O-Si substituted with a hydroxyl group.
• modified silicone oil having these side chains chlorinated or being modified by introducing an amino group, epoxy group, polyether group, carboxyl group, hydroxyl group, trifluoroalkyl group, alcohol ester group, alkyl group or the like.
• the silicone dispersion is a dispersion in which silicone resin or silicone rubber at an initial stage of polymerization has been dissolved in a solvent, and it forms a film having a three-dimensional network structure through condensation upon heating.
• organopolysiloxanes can be used without limitation to those enumerated above.
• the commercial products include SH200, PRX413, SH8011 and SD8000 (manufacture by Toray Dow Corning Silicone Co., Ltd.), KP-801M, KPN-3504 (manufactured by Shin-Etsu Chemical Co., Ltd.).
• the amount of organopolysiloxane incorporated may be from about 0.05 to about 10 % by weight, preferably from about 0.5 to 5 % by weight, based on the treatment agent of the present invention.
• Stain preventing agents, UV absorbents, surface active agents, disinfectants, insecticides, antistatic agents, perfumes or the like as described in Japanese Patent Kokoku Publication Nos. 6163/1987 and 33797/1988 may be added to the treatment agent of the present invention according to necessity.
• an antistatic agent, an aminoplast resin, an acrylic polymer, a natural wax, a silicone resin or the like may further be added in such amounts that the effect of the present invention is not inhibited.
• the treatment agent in particular the water and oil repellent of the present invention may be composed of aqueous emulsion-type composition prepared by the emulsion polymerization method.
• the water and oil repellent of the present invention can be applied to a substrate according to a conventionally known method.
• a method of dispersing said water and oil repellent into an organic solvent or water to dilute it, attaching it on the surface of the substrate by a procedure such as dip application, spray application, foam application to the substrate and the like, and drying it is usually adopted.
• the drying may be carried out by allowing to stand (solar drying or shade drying) at room temperature (0 to 30°C) or by heat-drying with a household dryer, an iron and a drier. If necessary, the curing may be also carried out by applying the water and oil repellent together with an appropriate closslinking agent.
• mothproofing agents in addition to the water and oil repellent of the present invention, mothproofing agents, softening agents, antimicrobial agents, flame-retardants, antistatic agents, paint primers and crease-retardants can also be added and used in combination.
• concentration of the copolymer in the treatment liquid may be from 0.05 to 10% by weight.
• concentration of the copolymer in the treatment liquid may be from 0.1 to 5% by weight.
• the water and oil repellent may be in the form of emulsion, aerosol, solid or paste.
• the water and oil repellent may be used in a water and oil repellent product or article.
• the water and oil repellent product may comprise, for example (a) a water and oil repellent alone, (b) a water and oil repellent and an application apparatus, or (c) a water and oil repellent and a container in which the water and oil repellent is contained.
• the water and oil repellent product which comprises a water and oil repellent emulsion may be for example (i) a water and oil repellent product comprising a water and oil repellent which is charged in a container equipped with a mechanism for spraying a liquid in said container outside (for example using a trigger type container); or (ii) a water and oil repellent product comprising a water and oil repellent which is charged in a container equipped with a mechanism for propelling a liquid in said container outside using a pressure (for example using a manual pump container or an aerosol type container). It may be also a water and oil repellent product in the form of foam comprising the emulsion containing additionally a foaming agent which is charged in the container of (i) or (ii).
• examples of the foaming agent which is added to the emulsion are preferably an anionic surfactant, a cationic surfactant, an amphoteric surfactant or a nonionic surfactant which has the foaming property previously known.
• anionic surfactant for example, sodium alkyl aryl sulfonate salt, sodium alkyl sulfuric ester salt, sodium alkyl sulfonate, sodium dialkyl sulfosuccinate, sodium polyoxyethylene alkyl aryl ether sulfuric ester, sodium polyoxyethylene alkyl ether sulfuric ester, sodium perfluoroalkylamido-N-propionate salt and the like are preferred.
• alkyl aryl trimethyl ammonium chloride alkyl trimethyl ammonium chloride and alkyl dimethyl amine acetate salt are preferred.
• amphoteric surfactant for example, alkylbetaine and alkylimidazoline are preferred.
• nonionic surfactant for example, polyoxyethylene alkyl ether, polyoxyethylene alkyl aryl ether, polyoxyethylene fatty acid ester, polyoxyethylene alkylamide, polyoxyethylene lanolin alcohol, polyoxyethylene sorbitan fatty acid ester, polyoxyethylene sorbitol fatty acid ester, dimethylalkylamine oxide, bishydroxyethyl alkylamine oxide, N-alkylmorpholine oxide, polyoxyethylene fatty acid alkylolamide and sucrose ester are preferred.
• the foaming agent is preferably those which have the initial foam height of at least 30 mm at the concentration of the foaming surfactant of 0.1% by weight at 30°C when measuring according to the foaming measurement method of JIS K-3362.
• the amount of the foaming surfactant is preferably from 0.007 to 2 parts by weight based on 100 parts by weight of the treatment agent of the present invention.
• the water and oil repellent is sprayed or coated to the substrate, or the substrate is dipped into the water and oil repellent using these water and oil repellent products.
• a coating apparatus such as a sponge, a roller or a brush may be used and these coating apparatuses may be equipped in the container.
• the water and oil repellent in the form of solid or paste is applied to the substrate.
• the water and oil repellent product which comprises the water and oil repellent in the form of solid may be charged in a stick type container such that being used for a lipstick or in a box type container such that being used for car wax.
• the water and oil repellent product which comprises the water and oil repellent in the form of paste may be charged in a tube type container such that being used for a dentifrice or in a box type container such that being used for car wax.
• an application apparatus such as a sponge, a roller or a brush may be used and these application apparatuses may be equipped in the container.
• the water and oil repellent of the present invention may be used as an aerosol.
• the water and oil repellent of the present invention can easily form the aerosol by adding a propellant to the stock liquid and charging in a container.
• a propellant liquid petroleum gas (LPG), propane, butane, dimethyl ether, carbon dioxide, nitrogen gas and the like can be used.
• LPG liquid petroleum gas
• propane, butane, dimethyl ether, carbon dioxide, nitrogen gas and the like can be used.
• an alternative fluorocarbon such as HFC-134a and HCFC-141b is also used.
• the weight ratio of the stock liquid to the propellant is from 99.5/0.5 to 30/70, and preferably from 99/1 to 50/50.
• a substrate to be treated with the water and oil repellent of the present invention is preferably a textile.
• the textile various examples can be recited. Examples of them include an animal- and vegetative-origin natural fiber such as cotton, hemp, wool and silk; a synthetic fiber such as a polyamide, a polyester, polyvinyl alcohol, polyacrylonitrile, polyvinyl chloride and polypropylene; a semi-synthetic fiber such as rayon and acetate; an inorganic fiber such as glass fiber, carbon fiber and asbestos fiber; or a mixture of these fibers.
• an animal- and vegetative-origin natural fiber such as cotton, hemp, wool and silk
• a synthetic fiber such as a polyamide, a polyester, polyvinyl alcohol, polyacrylonitrile, polyvinyl chloride and polypropylene
• a semi-synthetic fiber such as rayon and acetate
• an inorganic fiber such as glass fiber, carbon fiber and asbestos fiber; or a mixture of these fibers.
• the textile may be any of in the form of yarn, fabric and the like.
• the substrate which can be treated with the water and oil repellent of the present invention include glass, paper, wood, leather, fur, asbestos, brick, cement, metal and metal oxide, ceramics (e.g. tile), plastic, coating surface and plaster, rubber, cork and the like, in addition to a textile.
• Examples of the substrate to be treated include:
• Water repellency and oil repellency shown in the Examples and Comparative Examples are expressed by the following evaluations.
• Water repellency is expressed in terms of water repellency No. (see Table 1 below) by a spray method in accordance with JIS (Japanese Industrial Standard) L-1092.
• Oil repellency is expressed in terms of oil repellency No. by observing the state whether the drop can be maintained on the cloth for 30 seconds after one drop (about 5 mm in diameter) of a test solution shown in Table 2 below is placed on a sample cloth (AATCC TM118-1992).
• the symbol "+" assigned to water repellency No. indicates slightly good performance and the symbol "-" indicates slightly poor performance.
• This emulsion was transferred to a flask equipped with a stirrer, a thermometer and a reflux condenser, nitrogen purge was conducted sufficiently at 60°C, and then 0.3 g of ammonium persulfate was added to initiate the polymerization. At 10 hours after the initiation of polymerization, it was confirmed that 99% of U1 had reacted by gas chromatography and an emulsion having the solid content of 30% was obtained.
• This emulsion was transferred to a flask equipped with a stirrer, a thermometer and a reflux condenser, nitrogen purge was conducted sufficiently at 60°C, and then 0.3 g of ammonium persulfate was added to initiate the polymerization. At 10 hours after the initiation of polymerization, it was confirmed that 99% of the monomer b had reacted by gas chromatography and an emulsion having the solid content of 30% was obtained.
• Emulsion polymerization was carried out in the same manner as in Preparative Example 5 using the monomer U3 (a urethane bond-containing monomer) instead of the monomer U2 to give an emulsion having the solid content of 30%.
• This emulsion was transferred to a flask equipped with a stirrer, a thermometer and a reflux condenser, nitrogen purge was conducted sufficiently at 60°C, and then 0.3 g of ammonium persulfate was added to initiate the polymerization. At 10 hours after the initiation of polymerization, it was confirmed that 99% of the monomer b had reacted by gas chromatography and an emulsion having the solid content of 30% was obtained.
• Each of the water and oil repellents obtained in Preparative Examples 4 to 6 were diluted with water so as to have solid content of 3% and this liquid was uniformly sprayed on a white cotton broad cloth, a white polyester/cotton-blended broad cloth, a white polyester tropical cloth, a white nylon taffeta cloth so as to be 100 g/m 2 . Spray was carried out using a hand spray. Then, these cloths were dried at room temperature for 24 hours. The water and oil repellency test was carried out for these treated cloths. The test results are shown in Table 5.
• This emulsion was transferred to a flask equipped with a stirrer, a thermometer and a reflux condenser, nitrogen purge was conducted sufficiently at 60°C, and then 0.1 g of 2,2'-azobis(2-amidinopropane)dihydrochloride was added to initiate the polymerization. At 5 hours after the initiation of polymerization, it was confirmed that 99% of X1 had reacted by gas chromatography and an emulsion having the solid content of 10% was obtained.
• This emulsion was transferred to a flask equipped with a stirrer, a thermometer and a reflux condenser, nitrogen purge was conducted sufficiently at 60°C, and then 0.3 g of 2,2'-azobis(2-amidinopropane)dihydrochloride was added to initiate the polymerization. At 5 hours after the initiation of polymerization, it was continued that 99% of the monomer b had reacted by gas chromatography and an emulsion having the solid content of 30% was obtained.
• This emulsion was transferred to a flask equipped with a stirrer, a thermometer and a reflux condenser, nitrogen purge was conducted sufficiently at 60°C, and then 0.3 g of 2,2'-azobis(2-amidinopropane)-dihydrochloride was added to initiate the polymerization. At 5 hours after the initiation of polymerization, it was confirmed that 99% of the monomer b had reacted by gas chromatography and an emulsion having the solid content of 30% was obtained.
• This emulsion was transferred to a flask equipped with a stirrer, a thermometer and a reflux condenser, nitrogen purge was conducted sufficiently at 60°C, and then 0.3 g of 2,2'-azobis(2-amidinopropane)dihydrochloride was added to initiate the polymerization. At 5 hours after the initiation of polymerization, it was confirmed that the monomer b of 99% had reacted by gas chromatography and an emulsion having the solid content of 30% was obtained.
• This emulsion was transferred to a flask equipped with a stirrer, a thermometer and a reflux condenser, nitrogen purge was conducted sufficiently at 60°C, and then 0.3 g of 2,2'-azobis(2-amidinopropane)dihydrochloride was added to initiate the polymerization. At 5 hours after the initiation of polymerization, it was confirmed that 99% of the monomer b had reacted by gas chromatography and an emulsion having the solid content of 30% was obtained.
• This emulsion was transferred to a flask equipped with a stirrer, a thermometer and a reflux condenser, nitrogen purge was conducted sufficiently at 60°C, and then 0.5 g of 2,2'-azobis(2-amidinopropane)dihydrochloride was added to initiate the polymerization. At 5 hours after the initiation of polymerization, it was confirmed that 99% of the monomer b had reacted by gas chromatography and an emulsion having the solid content of 15% was obtained.
• Emulsion polymerization was carried out in the same manner as in Preparative Example 16 using X3 (a urethane bond-containing monomer, 66.7% di-n-butyl adipate solution) synthesized in Preparative Example 9 instead of X2 (a urethane bond-containing monomer, 66.7% di-n-butyl adipate solution) synthesized in Preparative Example 8 to give an emulsion having the solid content of 15%.
• X3 a urethane bond-containing monomer, 66.7% di-n-butyl adipate solution
• X2 a urethane bond-containing monomer, 66.7% di-n-butyl adipate solution
• Emulsion polymerization was carried out in the same manner as in Preparative Example 16 using X4 (a urethane bond-containing monomer, 66.7% di-n-butyl adipate solution) synthesized in Preparative Example 10 instead of X2 (a urethane bond-containing monomer, 66.7% di-butyl adipate solution) synthesized in Preparative Example 8 to give an emulsion having the solid content of 15%.
• X4 a urethane bond-containing monomer, 66.7% di-n-butyl adipate solution
• X2 a urethane bond-containing monomer, 66.7% di-butyl adipate solution
• compositions (the water and oil repellents) obtained in Preparative examples 11 to 17 and Comparative Preparative Example 2
• the following evaluation was carried out.
• Each of the water and oil repellents obtained in Preparative Examples 11 to 17 and Comparative Preparative Example 2 was diluted with ion-exchanged water so as to have solid content of 4% and this liquid was charged in an aerosol can. CO 2 as a propellant was further charged thereto and the container was sealed. The weight ratio of the water and oil repellent to the propellant was 50/50.
• the aerosol was uniformly sprayed on a white cotton broad cloth, a white polyester/cotton-blended broad cloth, a white polyester tropical cloth and a white nylon taffeta cloth so as to be 100 g/m 2 , and then these cloths were dried at room temperature for 24 hours. The water and oil repellency test was carried out for these treated cloths. The test results are shown in Tables 8 and 9.
• the treatment agent in the form of foam was placed on a white cotton broad cloth, a white polyester/cotton-blended broad cloth, a white polyester tropical cloth and a white nylon taffeta cloth, uniformly applied with a sponge so as to be 100 g/m 2 , and then these cloths were dried at room temperature for 24 hours.
• the water and oil repellency test were carried out for these treated cloths. The test results are shown in Tables 8 and 9.
• composition of the present invention is superior in processability at low temperature and a property of forming a smooth film.

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